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Respiratory Disease

Respiratory disease affects respiratory organs such as nasal cavity, pharynx, larynx, trachea, bronchus, lung, thorax, diaphragm.
Typical respiratory infections include colds and influenza, bronchitis, and pneumonia.

Respiratory Disease

COVID-19

STANDARD M nCoV Real-Time Detection kit


FDA EUA Approved 
KOREA MFDS Approved 
STANDARD M nCoV Real-Time Detection kit is used for rapid identification and detection of novel coronavirus (2019-nCoV) nucleic acids in human nasopharyngeal swabs and throat swab samples.

STANDARD Q COVID-19 Ag

 
WHO EUL
KOREA MFDS Approved
TGA Approved 
STANDARD Q COVID-19 Ag Test is a rapid chromatographic immunoassay for the qualitative detection of specific antigens to SARS-CoV-2 present in human nasopharynx.

STANDARD Q COVID-19 IgM/IgG Plus


KOREA MFDS Approved 
STANDARD Q COVID-19 IgM/IgG Plus Test kit is a rapid chromatographic immunoassay for the qualitative presumptive detection of specific IgM and IgG to 2019 novel coronavirus (nCoV) in humoral fluid.

STANDARD Q COVID-19 IgM/IgG Combo

 
STANDARD Q COVID-19 IgM/IgG Combo Test Kit is a rapid immunochromatography test designed for the qualitative presumptive detection of specific IgM and IgG to SARS-CoV-2 in humoral fluid.

STANDARD Q COVID-19 IgM/IgG Duo

 
STANDARD Q COVID-19 IgM/IgG Duo Test Kit is a rapid immunochromatography test designed for the qualitative presumptive detection of specific IgM and IgG to SARS-CoV-2 in humoral fluid.

STANDARD F COVID-19 Ag FIA

 
STANDARD F COVID-19 Ag FIA is the fluorescent immunoassay to detect SARS-CoV-2 infection in human nasopharyngeal swab specimen, identifying existence of SARS-CoV-2 viral nucleoprotein antigens.

STANDARD F COVID-19 IgM/IgG Combo FIA

 
STANDARD F COVID-19 IgM/IgG Combo FIA is the fluorescent immunoassay to detect the qualitative presumptive detection of specific IgM and IgG to 2019 novel coronavirus (nCoV) in humoral fluid.

STANDARD M Flu/SARS-CoV-2 Real-Time Detection kit


The STANDARD M Flu/SARS-CoV-2 Real-Time Detection Kit allows for ongoing flu surveillance while also testing for SARS-CoV-2 using Multiplex Real-Time RT PCR assay.

Influenza A&B

STANDARD F Influenza A/B FIA

This product performs qualitative analysis by detecting influenza virus A type and B type antigens in the nasopharyngeal sample.

STANDARD Q Influenza A/B (Q/F Device)

This product performs qualitative analysis by detecting influenza virus A type and B type antigens in the nasopharyngeal sample.

STANDARD Q Influenza A/B

This product performs qualitative analysis by detecting influenza virus A type and B type antigens in the nasopharyngeal sample.

RSV

STANDARD F RSV Ag FIA

This product performs qualitative analysis by detecting RSV antigens in the nasopharyngeal sample.

STANDARD Q RSV Ag (Q/F Device)

This product performs qualitative analysis by detecting RSV antigens in the nasopharyngeal sample.

STANDARD Q RSV Ag

This product performs qualitative analysis by detecting RSV antigens in the nasopharyngeal sample.

Strep A

STANDARD F Strep A Ag FIA

This product performs qualitative analysis by detecting Group A streptococcal antigens in samples.

STANDARD Q Strep A Ag

This product performs qualitative analysis by detecting Group A streptococcal antigens.

Legionella

STANDARD F Legionella Ag FIA

This product performs qualitative analysis by detecting Legionella Pneumophila antigens in the urine samples.

STANDARD Q Legionella Ag (Q/F Device)

This product performs qualitative analysis by detecting Legionella pnemophila antigens in urine.

S. pneumoniae

STANDARD F S.pneumoniae Ag FIA

This product performs qualitative analysis by detecting Streptococcus pneumoniae antigens in urine samples.

STANDARD Q S.pneumoniae Ag

This product performs qualitative analysis by detectiong Streptococcus pneumoniae antigen in urine.

Adeno Respi

STANDARD F Adeno Respi FIA

STANDARD F Adeno Respi FIA test (Analyzer+Test device) is a rapid diagnostic test that can use commercially.

STANDARD Q Adeno Respi Ag

STANDARD Q Adeno Respi Ag Test is an immunoassay that can identify the presence of Adenovirus antigens in respiratory specimens.

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